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It's evident to me that these individuals at the NIH don't want to find the real cause of ME/CFS, or maybe they're being told not to. My husband and I both have ME/CFS with immune deficiency and I can pinpoint exactly how and from whom I caught it and the exact date. Even though both of us have identical symptoms, all institutions refused to see us, i.e. Mayo and Cleveland clinics, the Undiagnosed Disease Network, etc. I finally started to understand what we had after I read your book as well as Neenyah Ostrom's book on ME/CFS. How can the medical community ignore this serious biomarker of immune deficiency??? It is non-hiv AIDs and it is easily transmissible, i.e. saliva can transmit it!! My heart sinks further and further as each year goes by and I see that most of the individuals studying this are all going down the wrong path. They're not looking for the pathogen. So frustrating and disappointing.

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